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维生素 D 类似物对自发性高血压大鼠心肌肥厚的治疗作用。

Therapeutic effects of vitamin D analogs on cardiac hypertrophy in spontaneously hypertensive rats.

机构信息

Laboratory of Metabolic Disease Research and Drug Development, Shengjing Hospital, China Medical University, Shenyang, China.

出版信息

Am J Pathol. 2010 Aug;177(2):622-31. doi: 10.2353/ajpath.2010.091292. Epub 2010 Jul 8.

Abstract

Vitamin D inhibits renin expression and blocks the compensatory induction of renin associated with the use of renin-angiotensin system inhibitors. Here we test the therapeutic effects of two commonly used vitamin D analogs and their combination with losartan on the development of left ventricular hypertrophy. One-month-old male spontaneously hypertensive rats were treated with vehicle, losartan, paricalcitol, doxercalciferol, a combination of losartan and paricalcitol, or a combination of losartan and doxercalciferol for 2 months. Blood pressure was markedly reduced by losartan, but not by paricalcitol or doxercalciferol alone. Echocardiograpy demonstrated a 65 to 80% reduction in left ventricular wall thickness with losartan, paricalcitol, or doxercalciferol monotherapy and almost complete prevention of left ventricular hypertrophy with the combination therapies. Attenuation of cardiac and cardiomyocyte hypertrophy, and suppression of atrial and brain natriuretic peptides, were most marked in the combination therapy groups. These changes were well correlated with left ventricular gene and microRNA expression profiles in the different treatment groups. Renal and cardiac renin expression was markedly increased in losartan-treated animals, but nearly normalized with combination therapy. The same vitamin D analogs suppressed plasma renin activity in patients receiving chronic hemodialysis. These data demonstrate that vitamin D analogs have potent antihypertrophic activity in part via suppression of renin in the kidney and heart, and combination of these analogs with losartan achieves much better therapeutic effects because of the blockade of the compensatory renin increase.

摘要

维生素 D 抑制肾素表达,并阻断肾素-血管紧张素系统抑制剂使用相关的肾素代偿性诱导。在此,我们测试了两种常用维生素 D 类似物及其与氯沙坦联合应用于左心室肥厚发展的治疗效果。将 1 月龄雄性自发性高血压大鼠用 vehicle、氯沙坦、帕立骨化醇、度骨化醇、氯沙坦与帕立骨化醇联合、或氯沙坦与度骨化醇联合进行 2 个月治疗。氯沙坦显著降低血压,但帕立骨化醇或度骨化醇单独使用则没有效果。超声心动图显示,氯沙坦、帕立骨化醇或度骨化醇单药治疗使左心室壁厚度降低 65%至 80%,联合治疗几乎完全预防左心室肥厚。联合治疗组心脏和心肌细胞肥大的衰减以及心房利钠肽和脑利钠肽的抑制作用最为明显。这些变化与不同治疗组左心室基因和 microRNA 表达谱密切相关。肾素和心肌肾素表达在接受氯沙坦治疗的动物中显著增加,但联合治疗后几乎恢复正常。相同的维生素 D 类似物也抑制了接受慢性血液透析患者的血浆肾素活性。这些数据表明,维生素 D 类似物具有强大的抗肥厚作用,部分是通过抑制肾脏和心脏中的肾素,而这些类似物与氯沙坦的联合应用由于阻断了代偿性肾素增加,从而实现了更好的治疗效果。

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